Optimization and Evaluation for the Capacitive Deionization Process of Wastewater Reuse in Combined Cycle Power Plants

Combined cycle power plants (CCPPs) use large amounts of water withdrawn from nearby rivers and generate wastewater containing ions and pollutants. Despite the need for wastewater reclamation, few technologies can successfully convert the wastewater into make-up water for CCPPs. Therefore, this study aimed to apply capacitive deionization (CDI) for wastewater reclamation in CCPPs. Using a bench-scale experimental unit, which included ion exchange membranes and carbon electrodes, response surface methodology (RSM) was used to optimize the operating conditions of the CDI process to increase the total dissolved solids (TDS) removal and product water ratio. The optimal conditions were found to be a voltage of 1.5 V, a flow rate of 15 mL/min, and an adsorption/desorption ratio of 1:0.8. The changes in CDI performance with time were also studied, and the foulants on the membranes, spacers, and electrodes were examined to understand the fouling mechanism. The TDS removal decreased from 93.65% to 55.70% after 10 days of operation due to the deposition of scale and organic matter. After chemical cleaning, the TDS removal rate recovered to 93.02%, which is close to the initial condition.


Introduction
Combined cycle power plants (CCPPs) account for over 80% of the world's electricity generation. Most of these plants use electric steam technology, which uses large amounts of water to produce steam that turns turbines to generate electricity. The blowdown from the steam cycle is typically quenched to 60 • C. To recycle this stream, a heat exchanger or chiller must be installed in the recycle path for reuse [1]. Combined heat and power plants combine two or more thermal cycles to increase the efficiency of energy use. A representative model is a mixture of a gas turbine cycle and a steam turbine cycle [2,3]. There are two major challenges with CCPPs. First, they use a large amount of pure water to operate the generator turbine and boiler. They also require cooling water to reduce the water temperature inside the plants [4,5]. Second, CCPPs generate wastewater that can harm the environment and human health if not properly treated. The high concentration of organic matter and hardness in the CCPP wastewater remaining in the operating system are the main causes of scale and fouling. This not only reduces the performance of the plant, but also degrades the quality of the treated water from the CCPPs and reduces the quantity of production. In addition, if it is used for irrigation, it can harm crops and make the soil less fertile [6][7][8]. As a result, discharge regulations for treated wastewater from CCPPs have become more stringent.

Principle of CDI
As one of the CDI types, membrane-coupled capacitive deionization (MCDI) was used in this work [46][47][48][49][50]. Ion removal by CDI is performed by repeating the ion adsorption and desorption phases [46][47][48][49][50][51][52]. Water is demineralized in an adsorption phase and Membranes 2023, 13, 316 3 of 20 the electrodes are regenerated in a desorption phase [8,50,53]. MCDI combines an ion exchange membrane on the electrode surface, reducing the influence of ions of the same charge and reducing the possibility of electrode fouling, resulting in better deionization performance [25,54,55]. CDI in this paper refers to MCDI. The principle of CDI is shown in Figure 1.

Principle of CDI
As one of the CDI types, membrane-coupled capacitive deionization (MCDI) wa used in this work [46][47][48][49][50]. Ion removal by CDI is performed by repeating the ion adsorp tion and desorption phases [46][47][48][49][50][51][52]. Water is demineralized in an adsorption phase an the electrodes are regenerated in a desorption phase [8,50,53]. MCDI combines an ion e change membrane on the electrode surface, reducing the influence of ions of the sam charge and reducing the possibility of electrode fouling, resulting in better deionizatio performance [25,54,55]. CDI in this paper refers to MCDI. The principle of CDI is show in Figure 1.

CDI Module
The lab-scale MCDI module consists of a few acrylic plates, a cathode, a cation e change membrane, a spacer, an anion exchange membrane, and an anode ( Figure 2). Th cathode and an anode made of activated carbon with a size of W100 × L100 mm 2 we purchased from Pureechem (Chungcheongbuk-do, South Korea). The adsorption capacit of the electrodes was 16 mg/g. The information about the pore volume and the surfac area was not disclosed because the manufacturer considers it confidential informatio The ion exchange membrane made of polyethylene with a size of W100 × L100 mm 2 , an the spacer made of polyethylene terephthalate with a size of W110 × L110 mm 2 were pr vided by Pureechem (Chungcheongbuk-do, South Korea) ( Table 1). The upper-left an center of the MCDI unit cell were punched at a size of 1 cm to allow the inflow and outflo water to flow, respectively. The top and bottom of the module had terminals (electric contacts) that were connected to the electrodes to apply electricity. Since the CDI proce was operated in constant voltage mode, the voltage was set to be constant while the cu rent changed.

CDI Module
The lab-scale MCDI module consists of a few acrylic plates, a cathode, a cation exchange membrane, a spacer, an anion exchange membrane, and an anode ( Figure 2). The cathode and an anode made of activated carbon with a size of W100 × L100 mm 2 were purchased from Pureechem (Chungcheongbuk-do, South Korea). The adsorption capacity of the electrodes was 16 mg/g. The information about the pore volume and the surface area was not disclosed because the manufacturer considers it confidential information. The ion exchange membrane made of polyethylene with a size of W100 × L100 mm 2 , and the spacer made of polyethylene terephthalate with a size of W110 × L110 mm 2 were provided by Pureechem (Chungcheongbuk-do, South Korea) ( Table 1). The upper-left and center of the MCDI unit cell were punched at a size of 1 cm to allow the inflow and outflow water to flow, respectively. The top and bottom of the module had terminals (electrical contacts) that were connected to the electrodes to apply electricity. Since the CDI process was operated in constant voltage mode, the voltage was set to be constant while the current changed.     Figure 3 shows a schematic of an experimental apparatus for the CDI process. A pump was used to supply feed water to the CDI module, and a power supply was used to apply voltage to the CDI electrode. The conductivity sensor was connected to a computer for real-time measurement and data collection. An electrode and ion exchange membrane were used after being immersed in ultrapure water for 2 h or more to remove contaminants from surface pores to secure an adsorption site. In addition, adsorption and desorption operations were performed for at least one cycle to achieve concentration equilibrium by an electrical force.    In the adsorption phase, the electrodes were charged to a given voltage, and ions of the opposite charge were attracted to the electrodes. In the desorption phase, the electrodes were switched to a negative potential, which caused the ions to be released from the electrodes, and the ions were released to the feed water passing through the cell. Accordingly, the product water was obtained in the adsorption phase and the concentrate (brine) was generated in the desorption phase.
When the TDS removal decreased to less than 70%, the CDI unit was cleaned in cleanin-place (CIP) mode. When the cleaning began, the remaining feed water was drained and the tank containing cleaning chemicals was connected to the CDI unit. The cleaning was performed in the order of acid (1 mM HCl) and alkali (1 mM NaOH solution), and then all chemicals in the process were drained and sufficient flushing was performed using deionized water.

Feed Solution
Real wastewater effluent from a CCPP (referred to as CCPP 'A') in Korea was used as the feed water. Table 2 summarizes the wastewater quality and discharge standard. There are three types of wastewater from a CCPP: power generation wastewater, washing wastewater, and cooling wastewater, and the water quality (especially TDS) fluctuates with time depending on the mixing ratio of the wastewater streams. Therefore, two types of mixed wastewater samples were used in this work. To determine the optimum operating conditions, the high-TDS wastewater (referred to as F1) was used, which represents the worst-case scenario. To evaluate the long-term operating performance, the wastewater with low TDS (referred to F2) was used, which represents the normal operating conditions. The details of the water quality of the wastewater are summarized in Table 2. Since CDI was used to recycle the wastewater, the target water quality was set to the industrial water reuse standard rather than the discharge standard. Thus, the product water quality was compared to the reuse standard. The discharge standard and the industrial water reuse standard are also listed in Table 2. The central composite design method was used to derive the optimal operating conditions of the CDI [56][57][58]. Voltage (X 1 ), flow rate (X 2 ), and desorption ratio (X 3 ) were used as input variables (factor), and the TDS removal rate (Y 1 ) and production quantity (Y 2 ) were designed as output variables (response) using a commercial software (Design-Expert 12.0). Table 3 summarizes the factors and responses used in the RSM. The conversion formula for TDS is given by Equation (1) [59]: where k is a correction coefficient and EC (µS/cm) is an electrical conductivity. The formula of rejection (%) is given by Equation (2): where C 0 is the initial concentration of the feed water, and C is the concentration of product water. The production quantity (mL) of formula is given by Equation (3): where V is the flow rate (mL/min), t AD is the time of the adsorption time, and TC is the total cycle. The standard for 1 cycle was set as the sum of adsorption and desorption times, and the criterion of TC was 24 h. The energy consumption (kWh/m 3 ) of formula is given by Equation (4) [60]: where IV is the current-voltage product (kW), η is the fraction of energy actually recovered and reused to power another charging phase, t AD is the time of the adsorption time (h), t DE is the time of the desorption time (h), and Q is the flow rate of the product water (m 3 /h). Figure 3 shows a flow chart of the RSM for the optimization of the operating conditions for the CDI process. First, the objective of the optimization was clarified. The key variables, including factors (inputs) and responses (outputs), were then identified. The experimental design was then performed to determine the details of the experiments based on the central composite design (CCD) method. Using this experimental matrix, a series of experiments were conducted and the results were analyzed using the RSM regression method. In addition, ANOVA (analysis of variance) of the results was also performed to validate the regression models. When the ANOVA test failed, the experimental design was modified and the other steps were repeated. Otherwise, the regression model was considered valid. Using the regression model, optimal conditions were explored through both graphical and point optimization.
The R 2 value for the regression models obtained from RSM trials was calculated using the Design-Expert software. The models were also validated using ANOVA. The larger the value of F and the smaller the value of p, the more significant the corresponding coefficient term [56]. The value of p was lower than 0.05, indicating that the model may be considered to be statistically significant [57].

Field Emission Scanning Electron Microscopy (FE-SEM) and Energy Dispersive X-ray Spectrometer (EDS) Analysis
The foulants on the membrane surfaces, spacers, and the electrode were examined to provide detailed information on the morphology and composition of the fouling materials [61,62]. A field emission scanning electron microscope (FE-SEM) and an X-ray spectrometer (EDS) (JSM-7160F from JEOL LTD) were applied to each sample. Prior to analysis, the samples were completely dried and coated with platinum for 30-45 s.

X-ray Photoelectron Spectrometer (XPS) Analysis
An X-ray photoelectron spectrometer Escalab250 (XPS) (Thermo Scientific) was used to analyze inorganic compounds, elements, etc. This technique has the advantage of being able to measure the elemental composition as well as the chemical and electronic state of the atoms within a material [63].

Sample Analysis
The pH and conductivity data were collected in real time using a WTW Multi 3620 IDS. An inductively coupled plasma optical emission spectrometer (ICP-OES) (Agilent) and an ion chromatograph 5000+ (Thermo Scientific) were used for cation and anion analysis, respectively. Turbidity was determined using a 2100Q and TOC was analyzed using a Shimadzu TOC analyzer.

Effects of Operating Variables
Initially, the effect of voltage, flow rate, and adsorption/desorption ratio on TDS removal in the CDI process was investigated using the one-factor-at-a-time (OFAT) method. The F1 feed water was used for different operating conditions. Figure 4 shows the effect of voltage on TDS removal. The voltage was applied in increments of 0.3 V and ranged from 1.2 V to 1.8 V. The TDS removal was highest at 86.3% at 1.5 V. In general, higher voltage can result in higher TDS removal. However, the TDS removal decreased at 1.8 V because the electrolysis of water occurs above 1.5 V, resulting in a decrease in ion adsorption efficiency.

Flow Rate
The TDS removal at different flow rates is shown in Figure 5. The flow rate cond were set in increments of 5 mL/min, ranging from 10 mL/min to 20 mL/min. As the rate increased, the TDS removal decreased. For example, the highest TDS removal (9 was achieved at the highest flow rate of 20 mL/min. This is due to a decrease in co time as the flow rate increases.

Flow Rate
The TDS removal at different flow rates is shown in Figure 5. The flow rate conditions were set in increments of 5 mL/min, ranging from 10 mL/min to 20 mL/min. As the flow Membranes 2023, 13, 316 8 of 20 rate increased, the TDS removal decreased. For example, the highest TDS removal (94.3%) was achieved at the highest flow rate of 20 mL/min. This is due to a decrease in contact time as the flow rate increases.
(a) (b) Figure 4. The results of the applied voltage of the CDI: (a) Voltage was set in 0.3 V incremen 1.2 V to 1.8 V; (b) The TDS removal rate was the highest at 86.3% at 1.5 V.

Flow Rate
The TDS removal at different flow rates is shown in Figure 5. The flow rate cond were set in increments of 5 mL/min, ranging from 10 mL/min to 20 mL/min. As th rate increased, the TDS removal decreased. For example, the highest TDS removal ( was achieved at the highest flow rate of 20 mL/min. This is due to a decrease in c time as the flow rate increases. (a) (b) Figure 5. The results of the flow rate of the CDI: (a) Flow rate was set in 5 mL/min incremen 10 mL/min to 20 mL/min; (b) The TDS removal rate was the highest at 94.3% at 10 mL/min.

Ratio of Sorption Time
The ratio of desorption time to adsorption time was adjusted from 1:0.8 to 1.2 crements of 0.2, and the results are summarized in Figure 6. At the ratio of 1:1, th removal was the highest (86.3%). When the desorption time was shorter than the a tion time, the TDS removal decreased to 78.7%. This is because the ions adsorbed electrode are not sufficiently desorbed. When the desorption time was too long, th removal was also low due to the occurrence of electrode aging, pore structure chang by-product generation caused by the long desorption time.

Ratio of Sorption Time
The ratio of desorption time to adsorption time was adjusted from 1:0.8 to 1.2 in increments of 0.2, and the results are summarized in Figure 6. At the ratio of 1:1, the TDS removal was the highest (86.3%). When the desorption time was shorter than the adsorption time, the TDS removal decreased to 78.7%. This is because the ions adsorbed on the electrode are not sufficiently desorbed. When the desorption time was too long, the TDS removal was also low due to the occurrence of electrode aging, pore structure change, and by-product generation caused by the long desorption time.

Optimization of Capacitive Deionization in CCP under RSM
Although the OFAT approach is helpful for qualitatively understanding the ence of operating variables, it is inefficient for finding optimal conditions and is una reveal interactions among variables. Therefore, RSM was used to further optimize th erating variables for CDI. Table 4 shows the experimental design matrix and results Design-Expert. Twenty-one experimental conditions were identified and a series of l atory-scale experiments were conducted. The corresponding values for TDS remova sponse 1) and water production (Response 2) are also shown in Table 4. Table 4. Arrangement of response surface design.

Optimization of Capacitive Deionization in CCP under RSM
Although the OFAT approach is helpful for qualitatively understanding the influence of operating variables, it is inefficient for finding optimal conditions and is unable to reveal interactions among variables. Therefore, RSM was used to further optimize the operating variables for CDI. Table 4 shows the experimental design matrix and results from Design-Expert. Twenty-one experimental conditions were identified and a series of laboratory-scale experiments were conducted. The corresponding values for TDS removal (Response 1) and water production (Response 2) are also shown in Table 4. The RSM results for the TDS removal and water production are shown in Tables 5 and 6, respectively. The R 2 values for several regression models, using linear, 2FI, quadratic, and cubic models, were compared. The sequential and lack-of-fit p-values were also calculated. The results indicated that the quadratic model was the most suitable for TDS removal (Y 1 ), and the 2FI model was suitable for water production (Y 2 ).  Table 4, the TDS removal varied from 47% to 91% by changing the voltage, flow rate, and adsorption/desorption ratio. Based on these results, a regression equation was derived as given by Equation (5): Y 1 : TDS Removal X 1 : Voltage X 2 : Flow rate X 3 : Sorption ratio According to the ANOVA (analysis of variance) results (Table 7), the model F-value was 28.94 (p-value < 0.0001), which means that the model is significant. In addition, the lack-of-fit F-value was 2.31, so it can be concluded that the lack of fit is not significant. In addition, the coefficient of determination (R 2 ) was 0.9595, which is also sufficiently high. This indicates that the regression equation can be used to predict the TDS removed. The response surface and contour plots for TDS removal are shown in Figure 7, which allows the visualization of the effect of the input variables. Increasing the voltage increased the TDS removal, while increasing the flow rate decreased the TDS removal. Increasing the sorption ratio also resulted in decreased TDS removal. However, the dependence of TDS removal on these variables is not linear, indicating that there were interactions among the variables.

Water Production
Equation (6) was obtained to predict water production using the data in

Water Production
Equation (6) was obtained to predict water production using the data in Table 4: Y 2 : Water Production X 2 : Flow rate X 3 : Sorption ratio According to the results of ANOVA (analysis of variance) (Table 8), the F-value of the model was 248.67 (p-value < 0.0001), which means that the model is significant. The corresponding coefficient of determination R 2 was 0.9907. Contrary to the case of TDS removal, the voltage was found to have no effect on water production.  Figure 8 shows the response surface and contour plots for water production. An increase in flow rate resulted in an increase in water production, while an increase in sorption ratio resulted in a slight decrease in water production. As mentioned earlier, the water production was constant regardless of the voltage. As can be seen in the figure, the water production is almost linearly proportional to the flow rate.

Graphical Optimization
There are two criteria to consider for CDI operation in this work. First, the TDS removal should be greater than 80%, which is required for wastewater reclamation. Second, the water production should be greater than 10,000 mL. To explore the conditions to satisfy both criteria at the same time, graphical optimization was carried out as shown in Figure 9. Here, the yellow areas correspond to the conditions for meeting the criteria. On the other hand, the gray areas correspond to conditions where the required criteria were not met. The desired ranges for voltage, flow rate and sorption ratio were then identified. A point optimization was also performed to determine the optimum point. The asterisks

Graphical Optimization
There are two criteria to consider for CDI operation in this work. First, the TDS removal should be greater than 80%, which is required for wastewater reclamation. Second, the water production should be greater than 10,000 mL. To explore the conditions to satisfy both criteria at the same time, graphical optimization was carried out as shown in Figure 9.
Here, the yellow areas correspond to the conditions for meeting the criteria. On the other hand, the gray areas correspond to conditions where the required criteria were not met. The desired ranges for voltage, flow rate and sorption ratio were then identified. A point optimization was also performed to determine the optimum point. The asterisks (star marks) indicate the proposed optimum conditions, which correspond to the voltage of 1.5 V, the flow rate of 15 mL/min and the sorption ratio of 1:0.8. It should be noted that there are two major limitations to the RSM approach. The first is that RSM is a "black box" approach that lacks flexibility. If the model needs to be changed to describe something physically slightly different, a lot of work is required to develop a new model. The second limitation is that it is a local analysis. The response surface developed is invalid for regions other than the factor ranges studied. Accordingly, the RSM models developed here are limited to the conditions considered in this study.

Results of Product Water Quality Analysis
The summary of the product water quality from the experiment under the optimum conditions (the voltage of 1.5V, the flow rate of 15 mL/min, and the sorption ratio of 1:0.8) is shown in Table 9. The TDS removal was 86.31%, which is 7.14% higher than the target removal. The water quality standard for industrial water reuse was also met.

Long-Term Operation of CDI
Although the previous experiments allow the determination of the optimum conditions for TDS removal and water production, they were carried out within a few hours. Therefore, a long-term (up to 10 days) continuous operation of the CDI was performed to It should be noted that there are two major limitations to the RSM approach. The first is that RSM is a "black box" approach that lacks flexibility. If the model needs to be changed to describe something physically slightly different, a lot of work is required to develop a new model. The second limitation is that it is a local analysis. The response surface developed is invalid for regions other than the factor ranges studied. Accordingly, the RSM models developed here are limited to the conditions considered in this study.

Results of Product Water Quality Analysis
The summary of the product water quality from the experiment under the optimum conditions (the voltage of 1.5V, the flow rate of 15 mL/min, and the sorption ratio of 1:0.8) is shown in Table 9. The TDS removal was 86.31%, which is 7.14% higher than the target removal. The water quality standard for industrial water reuse was also met.

Long-Term Operation of CDI
Although the previous experiments allow the determination of the optimum conditions for TDS removal and water production, they were carried out within a few hours. Therefore, a long-term (up to 10 days) continuous operation of the CDI was performed to study the fouling behavior and to identify the main foulants using the F2.

Reduction in TDS Removal and Energy Consumption
The experiment was conducted on a laboratory scale for a total of 10 days on a 24-h basis. The average TDS removal decreased over time from 93.65% to 55.70% as shown in Figure 10. In addition to the average values, the maximum and minimum TDS removals are shown in Table 10.

Reduction in TDS Removal and Energy Consumption
The experiment was conducted on a laboratory scale for a total of 10 days on a 24-h basis. The average TDS removal decreased over time from 93.65% to 55.70% as shown in Figure 10. In addition to the average values, the maximum and minimum TDS removals are shown in Table 10.
Energy consumption was also calculated using equation (4) and the results are summarized in Table 10. Since the amount of water produced by the CDI process is constant (11.625 L/day), the denominator of equation (4) has a constant value regardless of time. On the other hand, the numerator of this equation is almost proportional to the amount of ions removed by the CDI, so it decreased over time due to a decrease in TDS removal. Accordingly, the calculated energy consumption, assuming no energy recovery, decreased from 3.51 kWh/m 3 to 1.93 kWh/m 3 during the 10-day operation. Assuming 100% energy recovery, it decreased from 0.62 kWh/m 3 to 0.18 kWh/m 3 . This is undesirable because the quality of the product water deteriorated over time. To further investigate these phenomena, a series of analyses were performed on the membrane surface, spacers and electrodes.

Results of SEM-EDS Analysis
SEM-EDS analysis was performed for the electrodes before and after the CDI experiments. Figure 11a shows the SEM images of the electrode before the experiment. The intact electrode was composed of particulate materials with porous structures. After the  Energy consumption was also calculated using equation (4) and the results are summarized in Table 10. Since the amount of water produced by the CDI process is constant (11.625 L/day), the denominator of equation (4) has a constant value regardless of time. On the other hand, the numerator of this equation is almost proportional to the amount of ions removed by the CDI, so it decreased over time due to a decrease in TDS removal. Accordingly, the calculated energy consumption, assuming no energy recovery, decreased from 3.51 kWh/m 3 to 1.93 kWh/m 3 during the 10-day operation. Assuming 100% energy recovery, it decreased from 0.62 kWh/m 3 to 0.18 kWh/m 3 . This is undesirable because the quality of the product water deteriorated over time. To further investigate these phenomena, a series of analyses were performed on the membrane surface, spacers and electrodes.

Results of SEM-EDS Analysis
SEM-EDS analysis was performed for the electrodes before and after the CDI experiments. Figure 11a shows the SEM images of the electrode before the experiment. The intact electrode was composed of particulate materials with porous structures. After the experiment, the cathode was found to be covered with foulants. This can be seen in Figure 11b. On the other hand, the anode did not have any significant fouling as shown in Figure 11c. The EDS spectra are consistent with the results of the SEM analysis. Compared with the EDS spectrum for the intact electrode (Figure 11d), the EDS spectrum for the used cathode (Figure 11e) shows the peaks for Ca (9.67%), Si (2.92%) and Mg (1.03%). On the contrary, the EDS spectrum for the used anode (Figure 11f) does not show many foreign elements except for small amounts of S (0.06%) and Cl (0.05%). These results suggest that the fouling of the electrode preferentially occurs on the cathode side. Since the cathode adsorbs positively charged ions such as Ca 2+ and Mg 2+ , it can be covered by the deposits formed by these ions and dissolved organic matter [64].
Membranes 2022, 12, x FOR PEER REVIEW 15 of 21 experiment, the cathode was found to be covered with foulants. This can be seen in Figure  11b. On the other hand, the anode did not have any significant fouling as shown in Figure  11c. The EDS spectra are consistent with the results of the SEM analysis. Compared with the EDS spectrum for the intact electrode (Figure 11d), the EDS spectrum for the used cathode (Figure 11e) shows the peaks for Ca (9.67%), Si (2.92%) and Mg (1.03%). On the contrary, the EDS spectrum for the used anode (Figure 11f) does not show many foreign elements except for small amounts of S (0.06%) and Cl (0.05%). These results suggest that the fouling of the electrode preferentially occurs on the cathode side. Since the cathode adsorbs positively charged ions such as Ca 2+ and Mg 2+ , it can be covered by the deposits formed by these ions and dissolved organic matter [64].
(e) (f) The ion exchange membranes were also examined using the SEM-EDS technique. Before the CDI experiment, the surfaces of the cation exchange membrane (CEM) and anion exchange membrane (AEM) were clean as shown in Figure 12a,b. After the experiment, the surfaces were covered with gel-like and thread-like deposits as shown in Figure  12c,d. The analysis of the deposits by EDS showed that the deposits on the CEM and AEM   The ion exchange membranes were also examined using the SEM-EDS technique. Before the CDI experiment, the surfaces of the cation exchange membrane (CEM) and anion exchange membrane (AEM) were clean as shown in Figure 12a,b. After the experiment, the surfaces were covered with gel-like and thread-like deposits as shown in Figure 12c,d. The analysis of the deposits by EDS showed that the deposits on the CEM and AEM were different. The intact CEM contained a small amount of S and Na and the intact AEM had a small amount of N and Cl (Figure 12e,f) due to their functional groups [65]. After the experiment, Ca (2.69%), N (2.23%), Mg (0.53%), and Si (0.12%) were mainly found on the used CEM (Figure 12g), while O (21.61%) and S (1.88%) were observed on the used AEM (Figure 12h). were different. The intact CEM contained a small amount of S and Na and the intact AEM had a small amount of N and Cl (Figure 12e,f) due to their functional groups [65]. After the experiment, Ca (2.69%), N (2.23%), Mg (0.53%), and Si (0.12%) were mainly found on the used CEM (Figure 12g), while O (21.61%) and S (1.88%) were observed on the used AEM (Figure 12h).   The spacers were also observed by SEM-EDS. As shown in Figure 13a,b, the spacers were blocked by the deposits after the CDI experiment. Based on the morphology, they were assumed to be inorganic scales. The EDS analysis in Figure 13c,d confirmed this. It was found that the deposits in the used spacer contained Ca (4.79%), Mg (10.25%) and silica (1.95%). The spacers were also observed by SEM-EDS. As shown in Figure 13a and Figure  13b, the spacers were blocked by the deposits after the CDI experiment. Based on the morphology, they were assumed to be inorganic scales. The EDS analysis in Figure 13c and Figure 13d confirmed this. It was found that the deposits in the used spacer contained Ca (4.79%), Mg (10.25%) and silica (1.95%).

Results of XPS Analysis
In addition to EDS, XPS was used to further analyze the compositions of the deposits in the spacer. Figure 14 shows the XPS spectrum of the spacer after the CDI experiment. There were peaks corresponding to Mg 1s, O 1s, N 1s, Ca 2p, C 1s and Si 2p. Among them, the peaks for Mg, Ca, and O were higher than the others. These results are consistent with the previous results of the EDS analysis.

Results of XPS Analysis
In addition to EDS, XPS was used to further analyze the compositions of the deposits in the spacer. Figure 14 shows the XPS spectrum of the spacer after the CDI experiment. There were peaks corresponding to Mg 1s, O 1s, N 1s, Ca 2p, C 1s and Si 2p. Among them, the peaks for Mg, Ca, and O were higher than the others. These results are consistent with the previous results of the EDS analysis. The spacers were also observed by SEM-EDS. As shown in Figure 13a and Figure  13b, the spacers were blocked by the deposits after the CDI experiment. Based on the morphology, they were assumed to be inorganic scales. The EDS analysis in Figure 13c and Figure 13d confirmed this. It was found that the deposits in the used spacer contained Ca (4.79%), Mg (10.25%) and silica (1.95%).

Results of XPS Analysis
In addition to EDS, XPS was used to further analyze the compositions of the deposits in the spacer. Figure 14 shows the XPS spectrum of the spacer after the CDI experiment. There were peaks corresponding to Mg 1s, O 1s, N 1s, Ca 2p, C 1s and Si 2p. Among them, the peaks for Mg, Ca, and O were higher than the others. These results are consistent with the previous results of the EDS analysis.    Figure 14. The XPS spectra of the deposits in the spacer.

Cleaning
Previous results have shown that inorganic scale containing Ca and Mg is the main cause of CDI fouling. Since they degrade the treated water quality of CDI and reduce water production, it is necessary to remove them during or after CDI operation. Considering the compositions of the foulants, 1 mM HCl and 1 mM NaOH solutions were used as cleaning agents. The cleaning was performed by applying the acidic and alkaline solutions sequentially when the TDS removal decreased to less than 70%. Figure 15 shows the changes in TDS removal by CDI with time and the effectiveness of cleaning. The average TDS removal was 93.65% on day 1 and decreased to 68.82% on day 7.

Cleaning
Previous results have shown that inorganic scale containing Ca and Mg is the main cause of CDI fouling. Since they degrade the treated water quality of CDI and reduce water production, it is necessary to remove them during or after CDI operation. Considering the compositions of the foulants, 1 mM HCl and 1 mM NaOH solutions were used as cleaning agents. The cleaning was performed by applying the acidic and alkaline solutions sequentially when the TDS removal decreased to less than 70%. Figure 15 shows the changes in TDS removal by CDI with time and the effectiveness of cleaning. The average TDS removal was 93.65% on day 1 and decreased to 68.82% on day 7. Figure 15. The variation of TDS removal rate over 7 days of 24 h per day operation and after cleaning at 8 days; The average TDS removal rate was 93.65% on day 1 and gradually fell to 68.82% on day 7. After cleaning processes, the TDS removal rate recovered to the initial level of 93.02%.
The average TDS removal was 93.65% on day 1 and decreased to 68.82% on day 7. One of the reasons for this degradation is the electro-oxidation in electrodes. Due to the operation of the cell at a high voltage of 1.5 V, the anode can be electro-oxidized, leading to a reduction in capacity via a loss of pore structure and changes in surface chemistry. The elemental analysis indicated an increase in oxygen content, which may be associated with the electro-oxidation. Nevertheless, it should be noted that the TDS removal was restored to the initial level of 93.02% after the chemical cleaning. If electro-oxidation occurs, then the changes in the electrode should be irreversible and cannot be reverted by the chemical cleaning. Accordingly, further works will be required to clearly investigate the effect of electro-oxidation on the CDI performance degradation. Moreover, it is also necessary to optimize the cleaning methods for the long-term operation of CDI in future studies.

Conclusions
In this study, the CDI process has been proposed for the treatment of wastewater from CCPPs. The effect of operating conditions such as voltage, flow rate, and adsorption/desorption time ratio on the TDS removal in CDI was analyzed using both OFAT and RSM approaches. At the optimum conditions (the voltage of 1.5 V, the flow rate of 15mL/min, and the sorption ratio of 1:0.8), the TDS removal was 86.31%, which meets the requirement for industrial water reuse. However, a long-term CDI test showed a significant decrease in TDS removal from 93.65% to 55.70% over 10 days. To identify the foulants, the anodes, cathodes, CEMs, AEMs, and spacers were analyzed using SEM-EDS and XPS. It was found that fouling did not occur on the anode but on the cathode. Foulants were also observed in the CEMs, AEMs and spacers and they mainly contained Ca, Mg and Si. Accordingly, inorganic foulants, which may be associated with the organic matter, seemed to be responsible for the deterioration of the CDI performance. After the CDI test, Figure 15. The variation of TDS removal rate over 7 days of 24 h per day operation and after cleaning at 8 days; The average TDS removal rate was 93.65% on day 1 and gradually fell to 68.82% on day 7. After cleaning processes, the TDS removal rate recovered to the initial level of 93.02%.
The average TDS removal was 93.65% on day 1 and decreased to 68.82% on day 7. One of the reasons for this degradation is the electro-oxidation in electrodes. Due to the operation of the cell at a high voltage of 1.5 V, the anode can be electro-oxidized, leading to a reduction in capacity via a loss of pore structure and changes in surface chemistry. The elemental analysis indicated an increase in oxygen content, which may be associated with the electro-oxidation. Nevertheless, it should be noted that the TDS removal was restored to the initial level of 93.02% after the chemical cleaning. If electro-oxidation occurs, then the changes in the electrode should be irreversible and cannot be reverted by the chemical cleaning. Accordingly, further works will be required to clearly investigate the effect of electro-oxidation on the CDI performance degradation. Moreover, it is also necessary to optimize the cleaning methods for the long-term operation of CDI in future studies.

Conclusions
In this study, the CDI process has been proposed for the treatment of wastewater from CCPPs. The effect of operating conditions such as voltage, flow rate, and adsorption/desorption time ratio on the TDS removal in CDI was analyzed using both OFAT and RSM approaches. At the optimum conditions (the voltage of 1.5 V, the flow rate of 15mL/min, and the sorption ratio of 1:0.8), the TDS removal was 86.31%, which meets the requirement for industrial water reuse. However, a long-term CDI test showed a significant decrease in TDS removal from 93.65% to 55.70% over 10 days. To identify the foulants, the anodes, cathodes, CEMs, AEMs, and spacers were analyzed using SEM-EDS and XPS. It was found that fouling did not occur on the anode but on the cathode. Foulants were also observed in the CEMs, AEMs and spacers and they mainly contained Ca, Mg and Si. Accordingly, inorganic foulants, which may be associated with the organic matter, seemed to be responsible for the deterioration of the CDI performance. After the CDI test, chemical cleaning was performed using the acid and alkali solutions, which could recover the TDS removal from 68.82% to 92.03%. This indicates that CDI fouling can be controlled by chemical cleaning.
The significance of this paper lies in the application of the CDI process to the reclamation of CCPP wastewater, which is currently discharged despite its potential for reuse. Accordingly, this paper can contribute to the reduction of water withdrawal in CCPPs by accelerating the adoption of wastewater reclamation by the CDI process. One of the findings in this paper is the occurrence of fouling during the long-term operation of the CDI process, which is attributed to inorganic scale and organic matter. Although a chemical cleaning procedure has been proposed in this study, it has not yet been fully optimized. Therefore, further work will be required to explore the optimal methods and conditions for mitigating CDI fouling. It will also be necessary to develop pre-treatment techniques for this CDI process.